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Reference Material
Reference documents and regulatory information relevant to ISO 17025 compliance.
ISO/IEC 17025:2017
Structured integration of ISO/IEC 17025:2017, providing a reference for testing and calibration laboratory requirements. The official ISO PDFs remain the primary authoritative source.
8 Management system requirements
8.9 Management Reviews (Option A)
The laboratory management shall review its management system at planned intervals to ensure its continuing suitability, adequacy, and effectiveness.

Reference Material
Reference documents and regulatory information relevant to ISO 17025 compliance.
- ISO/IEC 17025:2017
  Structured integration of ISO/IEC 17025:2017, providing a reference for testing and calibration laboratory requirements. The official ISO PDFs remain the primary authoritative source.
  - Foreword
  - Introduction
    This document establishes requirements for laboratories to ensure competence, confidence, and valid results, aligning with ISO 9001 principles. It emphasizes risk-based planning, cooperation, and harmonization of standards while outlining key terminology usage.
  - 1 Scope
    This document defines the general requirements for laboratory competence, impartiality, and consistent operation, applicable to all organizations conducting laboratory activities.
  - 2 Normative References
    This section lists documents that are referenced in the text as requirements. Dated references apply to specific editions, while undated references apply to the latest version, including amendments.
  - 3 Terms and Definitions
    This section defines the terms used in this document. It references ISO/IEC Guide 99 and ISO/IEC 17000, along with additional terms specific to this standard.
  - 4 General requirements
  - 5 Structural requirements
  - 6 Resource requirements
  - 7 Process requirements
  - 8 Management system requirements
    - 8.1 Options
      The laboratory shall establish, document, implement, and maintain a management system that ensures the consistent achievement of the requirements of this document, following either Option A or Option B.
    - 8.2 Management System Documentation (Option A)
      Laboratory management shall establish, document, and maintain policies and objectives to ensure competence, impartiality, and consistent operation of the laboratory.
    - 8.3 Control of Management System Documents (Option A)
      The laboratory shall control the documents, both internal and external, that relate to the fulfilment of this document.
    - 8.4 Control of Records (Option A)
      The laboratory shall establish and retain legible records to demonstrate fulfilment of the requirements in this document, implementing necessary controls for record management.
    - 8.5 Actions to Address Risks and Opportunities (Option A)
      The laboratory shall consider risks and opportunities associated with its activities to ensure the achievement of management system objectives, prevent failures, and drive improvement.
    - 8.6 Improvement (Option A)
      The laboratory shall identify and select opportunities for improvement and implement necessary actions to enhance its management system, activities, and customer service.
    - 8.7 Corrective Actions (Option A)
      The laboratory shall take appropriate corrective actions when a nonconformity occurs, ensuring effective resolution and prevention of recurrence.
    - 8.8 Internal Audits (Option A)
      The laboratory shall conduct internal audits at planned intervals to ensure conformance to its management system requirements and the requirements of this document.
    - 8.9 Management Reviews (Option A)
      The laboratory management shall review its management system at planned intervals to ensure its continuing suitability, adequacy, and effectiveness.
  - Annex A (Informative) Metrological Traceability
  - Annex B (Informative) Management System Options
    This annex provides additional information on the management system options available to laboratories, ensuring conformity to ISO 9001 while fulfilling the requirements of this document.

8.9 Management Reviews (Option A)

The laboratory management shall review its management system at planned intervals to ensure its continuing suitability, adequacy, and effectiveness.

8.9.1 Management System Review

The laboratory management shall review its management system at planned intervals to ensure its continuing suitability, adequacy, and effectiveness, including the stated policies and objectives related to the fulfilment of this document.

8.9.2 Inputs to Management Review

The inputs to management review shall be recorded and shall include information related to the following:

Changes in internal and external issues relevant to the laboratory.
Fulfilment of objectives.
Suitability of policies and procedures.
Status of actions from previous management reviews.
Outcome of recent internal audits.
Corrective actions.
Assessments by external bodies.
Changes in the volume and type of work or in the range of laboratory activities.
Customer and personnel feedback.
Complaints.
Effectiveness of any implemented improvements.
Adequacy of resources.
Results of risk identification.
Outcomes of the assurance of the validity of results.
Other relevant factors, such as monitoring activities and training.

8.9.3 Outputs from Management Review

The outputs from the management review shall record all decisions and actions related to at least:

The effectiveness of the management system and its processes.
Improvement of laboratory activities related to the fulfilment of the requirements of this document.
Provision of required resources.
Any need for change.